A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673505



Internal ID15410157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6458468..6459413hg38UCSC Ensembl
Innerchr17:6361788..6362733hg19UCSC Ensembl
Innerchr17:6302512..6303457hg18UCSC Ensembl
Innerchr17:6302512..6303457hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38946
hg19946
hg18946
hg17946
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519881
Supporting Variants
Samples
Known GenesPITPNM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673505
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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