A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519665



Internal ID18817946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:756558..767068hg38UCSC Ensembl
Innerchr12:865724..876234hg19UCSC Ensembl
Innerchr12:735985..746495hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3810511
hg1910511
hg1810511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035947
Supporting Variants
Samples
Known GenesWNK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519665
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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