A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615042



Internal ID7001931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131651605..131652756hg38UCSC Ensembl
Innerchr7:131651660..131652702hg38UCSC Ensembl
Outerchr7:131651551..131652811hg38UCSC Ensembl
chr7:131336364..131337515hg19UCSC Ensembl
Innerchr7:131336419..131337461hg19UCSC Ensembl
Outerchr7:131336310..131337570hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12972202
SamplesNA18572
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615042
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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