A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662119



Internal ID18960400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122173126..122259649hg38UCSC Ensembl
Innerchr7:121813180..121899703hg19UCSC Ensembl
Innerchr7:121600416..121686939hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3886524
hg1986524
hg1886524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034624
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662119
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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