A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615432



Internal ID6655631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149609384..149643622hg38UCSC Ensembl
Innerchr7:149609384..149643622hg38UCSC Ensembl
Outerchr7:149608884..149644122hg38UCSC Ensembl
chr7:149306475..149340713hg19UCSC Ensembl
Innerchr7:149306475..149340713hg19UCSC Ensembl
Outerchr7:149305975..149341213hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3834239
hg1934239
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13003971
SamplesNA20872
Known GenesZNF767
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615432
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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