A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137210



Internal ID18905647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:36513125..36513183hg38UCSC Ensembl
Outerchr7:36552732..36552790hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975223, nssv3957827
SamplesKWS2, KWS1
Known GenesAOAH
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137210
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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