A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763361



Internal ID18968532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:9405969..9406024hg38UCSC Ensembl
Outerchr2:9546098..9546153hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077689
Supporting Variants
SamplesKWP1
Known GenesITGB1BP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763361
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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