A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705765



Internal ID15095731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88954166..88957970hg38UCSC Ensembl
Innerchr7:88583480..88587284hg19UCSC Ensembl
Innerchr7:88421416..88425220hg18UCSC Ensembl
Innerchr7:88228131..88231935hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg383805
hg193805
hg183805
hg173805
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515995
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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