A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710806



Internal ID15658076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16000927..16047835hg38UCSC Ensembl
Innerchr1:16327422..16374330hg19UCSC Ensembl
Innerchr1:16200009..16246917hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3846909
hg1946909
hg1846909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545627
Supporting Variants
Samples
Known GenesC1orf64, CLCNKA, CLCNKB, HSPB7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710806
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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