A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3495932



Internal ID18736887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112485649..112517599hg38UCSC Ensembl
Innerchr1:113028271..113060221hg19UCSC Ensembl
Innerchr1:112829794..112861744hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3831951
hg1931951
hg1831951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008375
Supporting Variants
Samples
Known GenesWNT2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3495932
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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