A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186173



Internal ID20753213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16754001..16845400hg38UCSC Ensembl
chr17:16657315..16748714hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3891400
hg1991400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497519
Supporting Variants
Samples
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.31644


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