A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764999



Internal ID17793033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155658453..155664329hg38UCSC Ensembl
Innerchr3:155376242..155382118hg19UCSC Ensembl
Innerchr3:156858936..156864812hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg385877
hg195877
hg185877
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv967244
Supporting Variants
SamplesHGDP00665
Known GenesPLCH1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764999
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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