A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638828



Internal ID7025613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64041459..64081871hg38UCSC Ensembl
Innerchr16:64041609..64081721hg38UCSC Ensembl
Outerchr16:64041309..64082021hg38UCSC Ensembl
chr16:64075363..64115775hg19UCSC Ensembl
Innerchr16:64075513..64115625hg19UCSC Ensembl
Outerchr16:64075213..64115925hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840413
hg1940413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15498595, essv15498598, essv15498587, essv15498589, essv15498591, essv15498592, essv15498583, essv15498597, essv15498600, essv15498601, essv15498586, essv15498584, essv15498594, essv15498599, essv15498588, essv15498602, essv15498582, essv15498596, essv15498590, essv15498603, essv15498585, essv15498581, essv15498593
SamplesHG03484, HG02628, NA19332, HG02852, NA20356, HG03095, NA19119, HG02922, HG03079, HG02573, NA18520, HG02545, HG03073, NA19043, HG03240, HG02010, HG02611, HG02814, HG03025, NA19093, HG02768, HG02676, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638828
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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