A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708637



Internal ID15655907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1753033..1780259hg38UCSC Ensembl
Innerchr1:1684472..1711698hg19UCSC Ensembl
Innerchr1:1674332..1701558hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3827227
hg1927227
hg1827227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545041
Supporting Variants
Samples
Known GenesNADK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708637
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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