A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655029



Internal ID18953310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4307501..4609833hg38UCSC Ensembl
Innerchr7:4347132..4649464hg19UCSC Ensembl
Innerchr7:4313658..4615990hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38302333
hg19302333
hg18302333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025419
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)nssv3655029
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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