A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892291



Internal ID22667339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39367524..39371877hg38UCSC Ensembl
chr6:39335300..39339653hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384354
hg194354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435591
Samples
Known GenesKIF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892291
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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