A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699963



Internal ID15089929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88909179..88914373hg38UCSC Ensembl
Innerchr7:88538493..88543687hg19UCSC Ensembl
Innerchr7:88376429..88381623hg18UCSC Ensembl
Innerchr7:88183144..88188338hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg385195
hg195195
hg185195
hg175195
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)nssv699963
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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