A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003654



Internal ID19092872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15347568..15451895hg38UCSC Ensembl
Innerchr2:15487692..15592019hg19UCSC Ensembl
Innerchr2:15405143..15509470hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38104328
hg19104328
hg18104328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3727914
Samples
Known GenesNBAS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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