A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771179



Internal ID19313590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7704039..7706040hg38UCSC Ensembl
chr1:7764099..7766100hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075535
Supporting Variants
SamplesKWP1
Known GenesCAMTA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771179
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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