A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027982



Internal ID19117200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119212310..119391719hg38UCSC Ensembl
Innerchr7:118852364..119031773hg19UCSC Ensembl
Innerchr7:118639600..118819009hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38179410
hg19179410
hg18179410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6596n100
Supporting Variantsnssv3751520, nssv3751521, nssv3751519, nssv3662070, nssv3662072, nssv3662071
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)nsv1027982
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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