A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038939



Internal ID19128158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52531827..52550411hg38UCSC Ensembl
Innerchr12:52925611..52944195hg19UCSC Ensembl
Innerchr12:51211878..51230462hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3818585
hg1918585
hg1818585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523593
Samples
Known GenesKRT71
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038939
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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