A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989588



Internal ID19231772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138718222..138718333hg38UCSC Ensembl
Outerchr7:138402967..138403078hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135987
Supporting Variants
SamplesKWS2
Known GenesATP6V0A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989588
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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