A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965855



Internal ID19241819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:148375771..148379231hg38UCSC Ensembl
Outerchr7:148072863..148076323hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383461
hg193461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130570
Supporting Variants
SamplesKWS2
Known GenesCNTNAP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965855
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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