A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177136



Internal ID20744176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16739101..16856000hg38UCSC Ensembl
chr17:16642415..16759314hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38116900
hg19116900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503157
Supporting Variants
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177136
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.35944


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