A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024801



Internal ID19114018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56678716..56709160hg38UCSC Ensembl
Innerchr7:56746409..56776853hg19UCSC Ensembl
Innerchr7:56713903..56744347hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3830445
hg1930445
hg1830445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661427, nssv3661426
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)nsv1024801
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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