A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487581



Internal ID22545497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63530550..63571662hg38UCSC Ensembl
chr2:63757684..63798796hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3841113
hg1941113
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833447
Supporting Variants
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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