A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710886



Internal ID16004842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16718016..16762555hg38UCSC Ensembl
Innerchr1:17044511..17089050hg19UCSC Ensembl
Innerchr1:16917098..16961637hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3844540
hg1944540
hg1844540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545667
Supporting Variants
Samples
Known GenesESPNP, LOC729574, MST1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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