A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497580



Internal ID18738535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:221958443..222072236hg38UCSC Ensembl
Innerchr1:222131785..222245578hg19UCSC Ensembl
Innerchr1:220198408..220312201hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38113794
hg19113794
hg18113794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014333
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)nssv3497580
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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