A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708596



Internal ID16002552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1479719..1518541hg38UCSC Ensembl
Innerchr1:1415099..1453921hg19UCSC Ensembl
Innerchr1:1404962..1443784hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3838823
hg1938823
hg1838823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545010
Supporting Variants
Samples
Known GenesATAD3A, ATAD3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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