A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023580



Internal ID19112797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13363906..13585350hg38UCSC Ensembl
Innerchr7:13403531..13624975hg19UCSC Ensembl
Innerchr7:13370056..13591500hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38221445
hg19221445
hg18221445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643135
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)nsv1023580
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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