A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515995



Internal ID15096602
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693176, nssv657359, nssv699413, nssv682035, nssv678833, nssv701076, nssv695014, nssv706123, nssv665637, nssv656682, nssv705765, nssv699983, nssv677430, nssv705622, nssv699963, nssv700639, nssv697246
Samples
Known GenesC7orf62, ZNF804B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515995
Frequency
Sample Size2026
Observed Gain5
Observed Loss13
Observed Complex0
Frequencyn/a


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