A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677430



Internal ID15067396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88519150..89880622hg38UCSC Ensembl
Innerchr7:88148465..89509936hg19UCSC Ensembl
Innerchr7:87986401..89347872hg18UCSC Ensembl
Innerchr7:87793116..89154587hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381361473
hg191361472
hg181361472
hg171361472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515995
Supporting Variants
Samples
Known GenesC7orf62, ZNF804B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677430
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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