A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975987



Internal ID18882586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:139348479..139348543hg38UCSC Ensembl
Outerchr7:139033225..139033289hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137296
Supporting Variants
SamplesKWS2
Known GenesC7orf55-LUC7L2, LUC7L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975987
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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