A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662145



Internal ID18960426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:125260003..125305497hg38UCSC Ensembl
Innerchr7:124900057..124945551hg19UCSC Ensembl
Innerchr7:124687293..124732787hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3845495
hg1945495
hg1845495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024270
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)nssv3662145
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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