A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463002



Internal ID22520887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73946227..73949976hg38UCSC Ensembl
chrX:73166062..73169811hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg383750
hg193750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873045
Supporting Variants
Samples
Known GenesJPX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463002
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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