A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980533



Internal ID18857738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71603875..71603964hg38UCSC Ensembl
Outerchr7:71068860..71068949hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143349
Supporting Variants
SamplesKWS1
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980533
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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