A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608684



Internal ID16396093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143558678..143865355hg38UCSC Ensembl
Innerchr7:143255771..143562448hg19UCSC Ensembl
Innerchr7:142965893..143193381hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38306678
hg19306678
hg18227489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1096533, nssv1096534
Samples
Known GenesCTAGE15, CTAGE6, FAM115A, FAM115C, LOC154761
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608684
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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