A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472972



Internal ID22530864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62010320..62074896hg38UCSC Ensembl
chr15:62302519..62367095hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3864577
hg1964577
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850782
Supporting Variants
Samples
Known GenesC2CD4A, VPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472972
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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