A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127963



Internal ID18925335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71701821..71701889hg38UCSC Ensembl
Outerchr7:71166806..71166874hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3587n106
Supporting Variantsnssv3957364
SamplesKWS1
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127963
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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