A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639963



Internal ID21832010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77957340..77957415hg38UCSC Ensembl
chrX:77212837..77212912hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106947
Supporting Variants
Samples
Known GenesATP7A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639963
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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