A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868807



Internal ID15816077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16768138..16814874hg38UCSC Ensembl
Innerchr17:16671452..16718188hg19UCSC Ensembl
Innerchr17:16612177..16658913hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3846737
hg1946737
hg1846737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574500
Supporting Variants
Samples
Known GenesCCDC144A, FAM106CP, USP32P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868807
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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