A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639300



Internal ID6679395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80920298..80965721hg38UCSC Ensembl
Innerchr16:80920349..80965671hg38UCSC Ensembl
Outerchr16:80920248..80965772hg38UCSC Ensembl
chr16:80954195..80999618hg19UCSC Ensembl
Innerchr16:80954246..80999568hg19UCSC Ensembl
Outerchr16:80954145..80999669hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3845424
hg1945424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv544e214
Supporting Variantsessv15535520, essv15535529, essv15535526, essv15535521, essv15535527, essv15535522, essv15535528, essv15535525, essv15535523, essv15535524
SamplesHG03455, NA19443, HG00335, NA19452, NA20276, NA19037, NA19331, NA19324, HG03157, NA19351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639300
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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