A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205699



Internal ID21344500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48964916..48964916hg38UCSC Ensembl
chrX:48822177..48822177hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933883
Supporting Variants
SamplesHG002
Known GenesKCND1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205699
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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