A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515646



Internal ID22573608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152892904..152936381hg38UCSC Ensembl
chrX:152061448..152104925hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3843478
hg1943478
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969208
Supporting Variants
Samples
Known GenesZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515646
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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