A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434237



Internal ID22492107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155803598..155984221hg38UCSC Ensembl
chrX:155033261..155213886hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38180624
hg19180626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871411
Supporting Variants
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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