A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6718



Internal ID15537145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:41257227..41277040hg38UCSC Ensembl
Outerchr17:39413479..39433292hg19UCSC Ensembl
Outerchr17:36667005..36686818hg18UCSC Ensembl
Outerchr17:36667005..36686818hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3819814
hg1919814
hg1819814
hg1719814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2050
Supporting Variants
SamplesNA12156
Known GenesKRTAP9-6, KRTAP9-7
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)nssv6718
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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