A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997841



Internal ID19157378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:71370499..71408004hg38UCSC Ensembl
Innerchr2:71597629..71635134hg19UCSC Ensembl
Innerchr2:71451137..71488642hg18UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3837506
hg1937506
hg1837506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3864n100
Supporting Variantsnssv3577294
Samples
Known GenesZNF638
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997841
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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