A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623845



Internal ID6664012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75000036..75002645hg38UCSC Ensembl
Innerchr10:75000036..75002645hg38UCSC Ensembl
Outerchr10:74999842..75002864hg38UCSC Ensembl
chr10:76759794..76762403hg19UCSC Ensembl
Innerchr10:76759794..76762403hg19UCSC Ensembl
Outerchr10:76759600..76762622hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382610
hg192610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863949, essv13863954, essv13863952, essv13863947, essv13863950, essv13863948, essv13863951, essv13863953, essv13863955
SamplesHG02339, HG03300, NA19197, HG03209, NA19172, NA19189, NA19395, HG03109, NA19324
Known GenesKAT6B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623845
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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