A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662097



Internal ID18960378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119930443..119995388hg38UCSC Ensembl
Innerchr7:119570497..119635442hg19UCSC Ensembl
Innerchr7:119357733..119422678hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3864946
hg1964946
hg1864946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022766
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)nssv3662097
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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