A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024001



Internal ID19113218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53118347..53171912hg38UCSC Ensembl
Innerchr7:53186040..53239605hg19UCSC Ensembl
Innerchr7:53153534..53207099hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3853566
hg1953566
hg1853566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6350n100
Supporting Variantsnssv3661281
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)nsv1024001
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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