A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764633



Internal ID17756033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37936620..37945108hg38UCSC Ensembl
Innerchr3:37978111..37986599hg19UCSC Ensembl
Innerchr3:37953115..37961603hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg388489
hg198489
hg188489
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv980087
Supporting Variants
SamplesHGDP00521
Known GenesCTDSPL
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764633
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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