A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3500285



Internal ID19087926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:207916673..207940386hg38UCSC Ensembl
Innerchr1:208090018..208113731hg19UCSC Ensembl
Innerchr1:206156641..206180354hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3823714
hg1923714
hg1823714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999483
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)nssv3500285
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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