A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516669



Internal ID22574632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69751660..69758868hg38UCSC Ensembl
chrX:68971504..68978712hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg387209
hg197209
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978780
Supporting Variants
Samples
Known GenesEDA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516669
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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