A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612638



Internal ID6999538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26549527..26565121hg38UCSC Ensembl
Innerchr7:26549527..26565121hg38UCSC Ensembl
Outerchr7:26549027..26565621hg38UCSC Ensembl
chr7:26589146..26604740hg19UCSC Ensembl
Innerchr7:26589146..26604740hg19UCSC Ensembl
Outerchr7:26588646..26605240hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3815595
hg1915595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1276e214
Supporting Variantsessv12710787
SamplesHG03905
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612638
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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