A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032883



Internal ID19122105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40400961..40449484hg38UCSC Ensembl
Innerchr7:40440560..40489083hg19UCSC Ensembl
Innerchr7:40407085..40455608hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3848524
hg1948524
hg1848524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6339n100
Supporting Variantsnssv3661211
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032883
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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