A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924735



Internal ID17233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207076854..207076991hg38UCSC Ensembl
chr2:207941578..207941715hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440117
Supporting Variants
Samples
Known GenesKLF7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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