A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752894



Internal ID19051175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13558304..13676438hg38UCSC Ensembl
Innerchr7:13597929..13716063hg19UCSC Ensembl
Innerchr7:13564454..13682588hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38118135
hg19118135
hg18118135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026929
Supporting Variants
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)nssv3752894
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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