A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181238



Internal ID20748278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41277005..41430682hg38UCSC Ensembl
chr17:39433257..39586934hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38153678
hg19153678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504427
Supporting Variants
Samples
Known GenesKRT31, KRT33A, KRT33B, KRT34, KRT37, KRTAP16-1, KRTAP17-1, KRTAP29-1, LOC100505782
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer