A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456125



Internal ID22514002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7720499..7720499hg38UCSC Ensembl
chrY:7588540..7588540hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965786
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456125
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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