A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024361



Internal ID18766894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53993970..54776794hg38UCSC Ensembl
Innerchr7:54061663..54844487hg19UCSC Ensembl
Innerchr7:54029157..54811981hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38782825
hg19782825
hg18782825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661310
Samples
Known GenesHPVC1, LOC285878, SEC61G, VSTM2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024361
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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