A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032422



Internal ID19121644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85785638..85874099hg38UCSC Ensembl
Innerchr7:85414954..85503415hg19UCSC Ensembl
Innerchr7:85252890..85341351hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3888462
hg1988462
hg1888462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6521n100
Supporting Variantsnssv3655180
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)nsv1032422
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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