A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998624



Internal ID19158160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185870737..185980705hg38UCSC Ensembl
Innerchr2:186735464..186845432hg19UCSC Ensembl
Innerchr2:186443709..186553677hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38109969
hg19109969
hg18109969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583270
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)nsv998624
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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