A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8682



Internal ID15535182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:7808715..7842215hg38UCSC Ensembl
OuterchrX:7776756..7810256hg19UCSC Ensembl
OuterchrX:7736756..7770256hg18UCSC Ensembl
OuterchrX:7586492..7619992hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg385938
hg195938
hg185938
hg175938
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6785
Supporting Variants
SamplesNA12156
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)nssv8682
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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