A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643160



Internal ID18941441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14785997..14810632hg38UCSC Ensembl
Innerchr7:14825622..14850257hg19UCSC Ensembl
Innerchr7:14792147..14816782hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3824636
hg1924636
hg1824636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024192
Supporting Variants
Samples
Known GenesDGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643160
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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