A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026324



Internal ID19115541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118067692..118094251hg38UCSC Ensembl
Innerchr7:117707746..117734305hg19UCSC Ensembl
Innerchr7:117494982..117521541hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3826560
hg1926560
hg1826560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6594n100
Supporting Variantsnssv3662052
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)nsv1026324
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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