A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173793



Internal ID15533567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21563013..21572998hg38UCSC Ensembl
Innerchr1:21889506..21899491hg19UCSC Ensembl
Innerchr1:21762093..21772078hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg389986
hg199986
hg189986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545736
Supporting Variants
SamplesNINDS_181
Known GenesALPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173793
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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