A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614616



Internal ID7001509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112214235..112253669hg38UCSC Ensembl
Innerchr7:112214245..112253660hg38UCSC Ensembl
Outerchr7:112214226..112253679hg38UCSC Ensembl
chr7:111854290..111893724hg19UCSC Ensembl
Innerchr7:111854300..111893715hg19UCSC Ensembl
Outerchr7:111854281..111893734hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3839435
hg1939435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1322e214
Supporting Variantsessv12929603, essv12929601, essv12929602
SamplesHG04076, HG04042, HG03733
Known GenesZNF277
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614616
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer