A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2643



Internal ID15540467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:41796879..41830212hg38UCSC Ensembl
Outerchr7:41836477..41869810hg19UCSC Ensembl
Outerchr7:41803002..41836335hg18UCSC Ensembl
Outerchr7:41609717..41643050hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386680
hg196680
hg186680
hg176680
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5716
Supporting Variants
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv2643
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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