A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609544



Internal ID6996465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74352497..74393835hg38UCSC Ensembl
Innerchr6:74352497..74393835hg38UCSC Ensembl
Outerchr6:74351997..74394335hg38UCSC Ensembl
chr6:75062213..75103551hg19UCSC Ensembl
Innerchr6:75062213..75103551hg19UCSC Ensembl
Outerchr6:75061713..75104051hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3841339
hg1941339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12429458
SamplesNA18967
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609544
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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