A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637078



Internal ID18588673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36927550..37025769hg38UCSC Ensembl
Innerchr5:36927652..37025871hg19UCSC Ensembl
Innerchr5:36963409..37061628hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3898220
hg1998220
hg1898220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029936
Supporting Variants
Samples
Known GenesNIPBL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3637078
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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