A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2762602



Internal ID17481270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191346443..191353939hg38UCSC Ensembl
Innerchr3:191064232..191071728hg19UCSC Ensembl
Innerchr3:192546926..192554422hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg387497
hg197497
hg187497
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965411
Supporting Variants
SamplesHGDP00998
Known GenesCCDC50
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2762602
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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