A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735922



Internal ID159588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10000..2781000hg38UCSC Ensembl
chrX:60001..2699041hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382771001
hg192639041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432327
Supporting Variants
Samples
Known GenesAKAP17A, ASMT, ASMTL, ASMTL-AS1, CD99, CD99P1, CRLF2, CSF2RA, DHRSX, GTPBP6, IL3RA, LINC00102, LINC00685, MIR3690, MIR3690-2, MIR6089-1, MIR6089-2, P2RY8, PLCXD1, PPP2R3B, SHOX, SLC25A6, XG, XGPY2, ZBED1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735922
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001886


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