A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137752



Internal ID19261822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:41635541..41635625hg38UCSC Ensembl
Outerchr1:42101212..42101296hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3963770, nssv3970166
SamplesKWS2, KWS1
Known GenesHIVEP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137752
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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