A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439151



Internal ID22497021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136217037..136219977hg38UCSC Ensembl
chrX:135299196..135302136hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg382941
hg192941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877295
Supporting Variants
Samples
Known GenesMAP7D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439151
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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