A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038695



Internal ID19127914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69909966..70080072hg38UCSC Ensembl
Innerchr13:70484098..70654204hg19UCSC Ensembl
Innerchr13:69382099..69552205hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38170107
hg19170107
hg18170107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713201
Samples
Known GenesKLHL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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