A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710887



Internal ID16004843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16722220..16776915hg38UCSC Ensembl
Innerchr1:17048715..17103410hg19UCSC Ensembl
Innerchr1:16921302..16975997hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3854696
hg1954696
hg1854696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545668
Supporting Variants
Samples
Known GenesLOC729574, MST1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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