A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025873



Internal ID19115090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124951379..125028369hg38UCSC Ensembl
Innerchr7:124591433..124668423hg19UCSC Ensembl
Innerchr7:124378669..124455659hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3876991
hg1976991
hg1876991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6607n100
Supporting Variantsnssv3662142
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)nsv1025873
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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