A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495964



Internal ID20869161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41135738..41144157hg38UCSC Ensembl
chr17:39291990..39300409hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg388420
hg198420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035473
Samples
Known GenesKRTAP4-6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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