A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710496



Internal ID15657766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14880515..15130423hg38UCSC Ensembl
Innerchr1:15207011..15456919hg19UCSC Ensembl
Innerchr1:15079598..15329506hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38249909
hg19249909
hg18249909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545591
Supporting Variants
Samples
Known GenesKAZN, TMEM51-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710496
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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