A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643198



Internal ID18941479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16337894..16418849hg38UCSC Ensembl
Innerchr7:16377519..16458474hg19UCSC Ensembl
Innerchr7:16344044..16424999hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3880956
hg1980956
hg1880956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031019
Supporting Variants
Samples
Known GenesISPD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643198
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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