A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706123



Internal ID15096089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89161295..89164885hg38UCSC Ensembl
Innerchr7:88790609..88794199hg19UCSC Ensembl
Innerchr7:88628545..88632135hg18UCSC Ensembl
Innerchr7:88435260..88438850hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg383591
hg193591
hg183591
hg173591
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)nssv706123
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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