A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642857



Internal ID18941138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8844447..9116407hg38UCSC Ensembl
Innerchr7:8884077..9156037hg19UCSC Ensembl
Innerchr7:8850602..9122562hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38271961
hg19271961
hg18271961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020577
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)nssv3642857
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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